Neonatal Comfort Seat Allowing Safe Lumbar Puncture and Minimizing Failure: a Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 68
- 主要终点
- First attempt LP success
研究概览
简要总结
A research trial which compares standard of care against employing a novel device for immobilization of babies undergoing upright LP, the present working name for the device is LP Comfort Seat (LPCS).
The research question is:
P: In late-preterm to term babies who are 0-28 days and undergoing LP for R/O Sepsis I: Is the LPCS more effective C: Than human/RN assisted upright positioning O: In generating a higher rate of first attempt LP success
Primary outcome measure is first attempt LP success (any evidence of CSF which is diagnostically useful by content and volume)
Secondary outcome measures could include
- A qualitatively unadulterated tap (no blood) although as you know this is hard to control even with perfect positioning and technique and single pass
- A difference in FLACC score as measure of overall pain/comfort between test and control
详细描述
Lay Description: Newborn babies who are unwell sometimes need to undergo a medical procedure known as a 'lumbar puncture' (also called 'spinal tap'). During this procedure, a needle is inserted at the base of the spine to extract fluid from the spinal column. This is most often done to determine if the baby has meningitis. The medical device presented here places the child's comfort and safety at the center of the spinal tap/ lumbar puncture experience and in doing increases the success of this otherwise stressful and technically challenging procedure. This is achieved by placing the child in a stable, firm, but comfortable position nearly eliminating patient motion which otherwise interferes with procedure success, and reduces the variability associated with a human assistant/holder
In the course of routine medical care of infants and young children, it may be necessary to conduct a procedure known as a 'lumbar puncture' or 'spinal tap' which involves insertion of a needle into the base of the spinal column in order to extract fluid for diagnostic purposes. The goal is to obtain a fluid sample with minimal trauma on the first attempt. The target space into which the operator is aiming to access this fluid is approx. 3 mm in diameter. First attempt failure rates range from 30-50%. A second try immediately following a first try, even if successful, leads to more trauma to the patient and often a sub-optimal sample (the "bloody tap") due to surrounding tissue/vascular disruption.
Many factors may contribute to first attempt success in this procedure:
- The clinical condition of the baby including hydration
- How well pain is controlled (assisting in the reduction of movement)
- The experience and confidence of the operator conducting the procedure and technique
- The experience of the assistant positioning the baby. This factor is generally accepted among clinicians as the most important factor contributing to procedure outcome and yet it is highly variable.
The lumbar puncture procedure may be conducted with the baby placed in a side-lying position. The side-lying position is most common, historically, as the patient seems to be more stable. However the alignment of the spine is often disrupted.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 0 Days 至 28 Days(Child)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Late preterm (34 + weeks) Gestational Age to Term (42+ weeks GA)
- •Weight of 2.5 - 5 kg
排除标准
- •Any contraindication to having a lumbar punture procedure
研究组 & 干预措施
Lumbar Puncture Comfort Seat Arm
This is the group that will have the lumbar puncture conducted in an upright sitting position assisted by the medical device
干预措施: A novel device for immobilization of babies undergoing upright LP, the present working name (non-proprietary) for the device is LP Comfort Seat (LPCS) (Device)
Standard of Care Arm
This is the group that will have the lumbar puncture conducted in an upright sitting position assisted by the human assistant which is present standard of care
干预措施: Standard of Care (SOC) (Other)
结局指标
主要结局
First attempt LP success
时间窗: Assessed at each procedure
Primary outcome measure is first attempt LP success (any evidence of CSF which is diagnostically useful by content and volume)
次要结局
- FLACC Score(Assessed at each procedure)
- Clear tap(Assessed at each procedure)
研究者
Joel Cox
Dr. Joel Cox, MD, FRCPC
Nova Scotia Health Authority
